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4790-81-2

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4790-81-2 Usage

Synthesis Reference(s)

Journal of Medicinal Chemistry, 30, p. 62, 1987 DOI: 10.1021/jm00384a011

Check Digit Verification of cas no

The CAS Registry Mumber 4790-81-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,7,9 and 0 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 4790-81:
(6*4)+(5*7)+(4*9)+(3*0)+(2*8)+(1*1)=112
112 % 10 = 2
So 4790-81-2 is a valid CAS Registry Number.
InChI:InChI=1/C8H6O2/c9-7-3-1-2-6-4-5-10-8(6)7/h1-5,9H

4790-81-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-benzofuran-7-ol

1.2 Other means of identification

Product number -
Other names 7-hydroxybenzo<b>furan

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:4790-81-2 SDS

4790-81-2Relevant articles and documents

One-Pot Generation of Benzynes from Phenols: Formation of Primary Anilines by the Deoxyamination of Phenols

Akai, Shuji,Ikawa, Takashi,Masuda, Shigeaki

, (2020/03/23)

Benzynes were selectively generated in situ from phenols and trapped regioselectively with potassium hexamethyldisilazide to form primary anilines following acidic workup. The direct conversion of a phenolic hydroxyl group into a free amino group is a useful method for the preparation of primary aryl amines that are hard to synthesize by using coupling reactions involving phenol derivatives with ammonia. Whereas reactions of ortho- and meta-substituted phenols produced meta-substituted anilines exclusively, those of para-substituted phenols provided ortho-silylanilines.

INHIBITORS OF BRUTON'S TYROSINE KINASE AND METHODS OF THEIR USE

-

Page/Page column 147, (2017/09/02)

The present disclosure is directed to compounds of formula I and methods of their use and preparation, as well as compositions comprising compounds of formula I.

COMPOUNDS AND METHODS FOR TREATING HIV INFECTIONS

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Paragraph 0378-0380, (2015/04/21)

The present invention is directed to novel nanomolar and picomolar inhibitors of HIV reverse transcriptase, pharmaceutical compositions therefrom and methods for inhibiting reverse transcriptase and treating HIV infections, especially included drug resistant strains of HIV-1 and HIV-2 and/or secondary disease states and/or conditions which occur as a consequence of HIV infection.

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